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HS Code |
209592 |
| Iupac Name | 3-oxopropyl acetate |
| Common Name | Acetoxyacetone |
| Molecular Formula | C5H8O3 |
| Molar Mass | 116.12 g/mol |
| Appearance | Colorless to yellowish liquid |
| Boiling Point | 192-194 °C |
| Density | 1.108 g/cm³ |
| Cas Number | 5975-74-4 |
| Pubchem Cid | 12048 |
| Melting Point | -40 °C |
| Solubility In Water | Miscible |
| Smiles | CC(=O)OCC(=O)C |
As an accredited Acetoxyacetone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Acetoxyacetone, 100g, supplied in a sealed amber glass bottle with tamper-evident cap and hazard labels for safe handling. |
| Shipping | Acetoxyacetone should be shipped in tightly sealed containers under cool, dry, and well-ventilated conditions. It must be protected from heat, moisture, and incompatible substances. Shipping must comply with relevant regulations for flammable and potentially hazardous chemicals, and appropriate hazard labels should be clearly displayed on the packaging. Handle with care. |
| Storage | Acetoxyacetone should be stored in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and incompatible substances such as strong oxidizers and bases. Store in a tightly closed container, preferably amber glass, to protect from moisture and light. Ensure proper labeling and keep away from direct sunlight. Use appropriate spill containment and follow all relevant safety regulations. |
Applications of Acetoxyacetone in Industrial ManufacturingAcetoxyacetone is a specialized organic compound utilized by various manufacturing sectors. Its functional acetyl and keto groups support distinct transformation steps in chemical synthesis, enabling production of advanced intermediates and final products. As a direct producer, we support downstream industries in pharmaceuticals, agrochemicals, fine chemicals, and high-performance materials, each with rigorous compliance demands and proprietary integration methods. 1. Active Pharmaceutical Ingredient (API) SynthesisIn pharmaceutical manufacturing, Acetoxyacetone acts as a key building block for β-diketone intermediates used in the synthesis of active compounds, especially within non-steroidal anti-inflammatory drugs, antivirals, and oncology molecule libraries. It enters condensation and cyclization steps, where raw material traceability and GMP control remain mandatory. The shifting demand for high-purity intermediates in line with strict ICH Q7A guidelines drives the compound’s clean handling and accurate dosing per compound synthesis route. The degree of acetylation controls molecular orientation and influences yield in pharma synthesis. Typical downstream routes require integration with automated reactor systems, inert gas blanketing, and multi-step solvent extraction. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingAcetoxyacetone supports large-scale agrochemical synthesis, mainly in the production of heterocyclic intermediates for fungicides, herbicides, and insecticides. The compound’s high reactivity benefits cyclization and Michael addition reactions under precise exothermic control. Industrial batch and continuous flow plants monitor dosing based on stoichiometric balance and catalyst efficiency. Compliance emphasizes ISO 9001 and REACH chemical safety data, with waste stream management for acetyl by-products. Downstream, the material integrates at initial ketone synthesis or follows activation by acidic or basic catalysts, followed by distillation or solvent stripping. Industry compliance standards
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3. Organic Pigment and Dye SynthesisThe textile and colorant industry utilizes Acetoxyacetone for the manufacture of high-performance organic pigments and specialty dyes. It enables introduction of acetyl and keto motifs, crucial in forming metal complex dyes and certain anthraquinone derivatives. Production lines require RSL (Restricted Substance List) compliance and strict control of by-product content to meet global textile safety standards. Mixing ratios directly impact chromophore stability and shade depth; ratio optimization aligns with pigment carrier type and downstream metallization steps. The compound is typically fed into reactors with pH and temperature regulation, paired with downstream filtration and drying units. Industry compliance standards
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4. Synthesis of Specialty Monomers and Polymer ModifiersManufacturers in advanced material sectors employ Acetoxyacetone in the development of specialty monomers and reactive modifiers for high-performance polymers. It plays a role in the formation of diketone-based crosslinkers and curing agents for resin systems used in electronics and automotive coatings. This application relies on rigorous QC aligned with ISO 14001 (environmental) and downstream customer audits. The precise proportioning impacts polymer flexibility, cure speed, and resin shelf life. Manufacturers incorporate the compound into resin pre-polymerization or post-functionalization steps, utilizing inline viscosity and molecular weight checks as production quality gates. Industry compliance standards
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5. High-Purity Laboratory Reagent ProductionProducers of certified laboratory reagents utilize Acetoxyacetone as a synthetic precursor in analytical kits and reference materials. It is essential for generating diketone-based derivatization agents used in HPLC, GC, and spectrophotometric assays. Product handling must comply with ISO/IEC 17025 calibration standards and hazardous chemical storage rules. Usage ratios are defined by precise stoichiometry in small-batch synthesis, while impurities are tightly controlled to support validation protocols. Batch integration occurs within laminar flow hoods and specialized glass reactors, with QC confirmation against NIST-traceable standards. Industry compliance standards
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Every day at our plant, we work with acetoxyacetone, a colorless, clear liquid that shows its true value through its performance in synthetic routes. Our Acetoxyacetone, CAS 3710-30-3, arrives in 98% minimum purity, handled with care and controlled closely from raw material to drum. A chemical like this, with the formula C5H8O3, finds its way into reaction tanks across very different projects—mostly pushed by R&D teams searching for yield, selectivity, or a reliable building block that opens up new chemistry.
Synthetic chemists like the enolizable nature of acetoxyacetone and the flexibility it brings. In our synthesis halls, we see demand from those working on heterocycle construction, especially where control over substituent placement can make or break a new active. Our acetoxyacetone attracts interest for work on pyrazoles, isoxazoles, and related systems. Compared to similar beta-diketones like acetylacetone, it swaps a methyl group for an acetoxy, which can modulate both reactivity and solubility—and brings out new options for reaction conditions.
Years of hands-on practice have shown how this oxygenated chain cuts down on unnecessary byproducts. Where acetylacetone might introduce background noise in the NMR from tautomeric forms, acetoxyacetone stays reliably clear. In catalysis development, formulators exploring ligands with specific donor profiles have come to us asking for batch consistency that resists atmospheric degradation. Our tight control over storage temperature and time from distillation helps keep each drum within a narrow spec—real-world feedback from process chemists drives us to tackle the small details others miss.
The production cycle for acetoxyacetone demands careful attention, starting with acetic anhydride and acetone processed through our hydrogen chloride-catalyzed pathway. Versatile, but also capricious, this chemical can hydrolyze or oxidize during poor storage. For us, limiting water and minimizing exposure to air are non-negotiable steps. Strict moisture testing—both in the plant and during final QC—has consistently proven its worth by reducing failed reactions at the client bench. This sort of vigilance doesn’t show up on a typical product data sheet, but our direct reports from pharmaceutical and specialty chemical labs remind us how even trace acid presence can derail a scale-up.
We ship acetoxyacetone only in fresh HDPE drums with argon purging, watching the temperature of our warehouses and delivering new batches within weeks of process. The market sometimes offers re-packed or aged material, but our in-house tracking keeps batches consistent, helping downstream technicians avoid troubleshooting headaches. After years of making and using our own acetoxyacetone in side projects, we cannot overstate how chemical freshness causes some of those “why did the yield drop” moments.
Using acetoxyacetone alongside common reagents, chemists notice the specific handling differences. Acetylacetone, for one, shares some traits but has a reputation for volatility and odor that lingers in production halls during scale-up. Acetoxyacetone, on the other hand, gives off a much more neutral profile and stays easier to contain when loaded into plant-scale reactors. Unlike methyl acetoacetate, acetoxyacetone tends to deliver a more controlled introduction of the acetoxy function—something medicinal and agrochemical chemists desire when aiming to modulate hydrogen bonding or polarity in a new lead scaffold.
On the plant floor, differences become plain in crystallization times and downstream separations. We routinely see acetoxyacetone helping customers avoid stubborn emulsions during aqueous workup, where less substituted diketones tend to linger in the wrong layer and steal valuable time from extraction staff. Our own QA teams often notice the clarity of isolated products—the absence of yellowing or persistent residuals—after switching to our carefully distilled batches. Process chemists at scale can skip a re-crystallization step, a direct gain from the particular set of side reactions acetoxyacetone manages to dodge.
We field questions from innovation managers monthly. Many aim to tweak the balance between cost and outcome, hoping to avoid dead ends that other reagents introduce in their synthesis plans. Acetoxyacetone, with its tailored balance between reactivity and selectivity, fits neatly into targeted heterocycle assembly lines. Case histories from our own pilot plant detail insertion into condensation reactions, both under acid and base-catalyzed conditions, to develop new key intermediates for fungicides or pharmaceutical APIs.
Some teams report better regioselectivity in annulation sequences with acetoxyacetone compared to more symmetric beta-diketones. We see it in the results: formation of key N-heterocycles that would have otherwise produced significant isomeric waste. Time and again, these practical benefits—lower waste, easier downstream processing, sharper selectivity—override minor cost differences against baseline ketones. Our synthesis engineers spend time one-on-one troubleshooting these reactions, and we hear first-hand how quality and batch uniformity cut down on waste disposal and costly reruns.
On the discovery side, chemists working with us often develop fragments for combinatorial synthesis or scaffold-hopping programs. In university collaborations, we have supplied acetoxyacetone for the assembly of libraries based on fused bicyclic systems, where the acetoxy group later transforms into more reactive handles. These stories rarely make marketing glossies, but they play out over months of experimentation with project timelines riding on the smallest improvements in conversion rates or selectiveness.
Service feedback loops drive many of our improvements. In one round of pilot development, a customer’s prefered ligand prep was failing with off-spec acetoxyacetone sourced from an unfamiliar supplier. Their yields rebounded using our more stable, freshly produced material. Small pH variances from trace acid impurities, picked up during sub-quality storage, had been stalling palladium-catalyzed C–N couplings. We keep tabs on downstream issues by testing actual synthesis routes during QC, rather than relying on routine assays alone.
Other reports highlight acetoxyacetone’s clear gains for manufacturing specialty polymers. Control over the acetoxy function simplifies subsequent post-polymerization modifications, especially where acid scavenging capacity or selectivity toward a certain monomer unit is needed. We have witnessed research houses promote our acetoxyacetone as a reliable starting point due to its lower rates of peroxide formation relative to some commercial diketones.
For us, the difference between chemical manufacturing and simple selling lies in our responsibility for each kilo we release. We source each precursor with full traceability, apply batch-based analytics, and routinely run our own staff training refreshers on safe handling and packaging. The list of problems we have helped solve through close technical relationships with our clients keeps growing. Too often, a minor change in feedstock or shift in storage leads to extended root-cause analyses that soak up time and money. By controlling each link in our chain, we keep our output stable—a direct payback we observe in high process reproducibility for our end users.
Every delivery of acetoxyacetone comes out of processes tested for stability and tracked for trace impurities through advanced spectroscopic means. On our filling line, QA staff capture real-time data to confirm specs and investigate lot-to-lot consistency, which allows our customers to skip batch pre-screening on their own. In instances where a project needs a custom concentration or tighter purity, our scale-up teams work alongside technical service reps to adjust parameters and guarantee the compound performs as needed.
Our R&D department doesn’t just watch global literature—they benchmark against our actual results and customer feedback. Acetoxyacetone’s dynamic nature keeps us disciplined. Changes in ambient humidity or slight shifts in temperature on the plant floor can impact purity, so we run regular audits on the entire storage system. Recurrent customer calls flagging minor off-odors or color shifts led us to overhaul our venting, re-dryers, and seal protocols over the last three years. These seemingly minor refinements closed off failure routes that had eaten into customer development budgets. On the production side, such tweaks help our own efficiency: more on-spec batches, less rework, leaner logistics.
Technical support learns continually from production experience. Years ago, plant chemists pushed for new analytical checks beyond GC/HPLC, so we added routine moisture titration and trace acid checks by Karl Fischer and potentiometry. Those details allowed us to eliminate types of off-batch failures and gave our partners increased confidence, especially where their own scale-up parameters might have yet to be finalized.
Reliability and environmental responsibility walk hand in hand here. Decision-makers at our client companies tell us their priorities, and our own environmental compliance teams monitor not only VOC emissions but also worker exposure and waste disposal. Acetoxyacetone hurdled regulatory review as a specialty intermediate in most regions, yet it still lands on planning radar for safe handling.
Plant managers hear about these regulations early, because a slip in chemical stewardship can draw regulatory attention and force a shutdown. We invest in effective vapor management, drum tracking, and documented SAP entries for each batch. Our real impact runs beyond regulatory compliance—by producing consistently high-purity acetoxyacetone in sealed, secure containers, we cut down on worker exposure and downstream waste. Our production routines have steadily dropped waste by 16% since 2021 through cycle time optimization and better off-gas management.
Customers value not just what acetoxyacetone does, but how it is produced. We care intensely who is going to use each drum, because these are not faceless commodities—they form the backbone of processes that put medicines and innovations into society. Environmental stewardship, accuracy, and hands-on technical dialogue define how we handle every kilo.
Our engagement with customers goes beyond order fulfillment: we walk through process instructions, solvent reuse options, and safe quenching or neutralization strategies. For instance, process engineers in the pilot plant stage report that replacing acetylacetone with acetoxyacetone can cut back cycle times and cleanroom re-clearing due to its lower volatility and less lingering odor.
Safety means full transparency over chemical handling. We provide detailed hazard training, participate in site audits, and invest in solvent vapor capture systems in our shipping area. It is common practice for our technical team to consult with procurement and R&D teams during cross-validation of our material, ensuring it functions not only on paper, but also on large reactors during actual production runs.
Every new customer exploration with acetoxyacetone turns into a case study for our teams. Batch histories logged into our systems give clear trails for comparison, and our research team circles back after new campaigns to compare conversions and yields against past results—this direct loop between production and application means any observed drift, either in reactivity or stability, guides our next cycle of improvement.
On the ground, production staff champion even minor successes: a cut in unexpected side reactions, a better reaction clean-up, and a quicker QA release mean less waste and stronger project outcomes for all parties. We make acetoxyacetone not as just a line-item product, but as a partnership offering, grounded in the daily routines and detailed feedback of people who make, transport, store, and ultimately transform this molecule into breakthroughs. Taking this partnership seriously, we keep to high standards in each bottle, ensuring chemists on the other end never have to wonder where the next variable in their process might appear.